Id |
Subject |
Object |
Predicate |
Lexical cue |
TextSentencer_T1 |
0-156 |
Sentence |
denotes |
A quantitative proteomic workflow for characterization of frozen clinical biopsies: laser capture microdissection coupled with label-free mass spectrometry. |
T1 |
0-156 |
Sentence |
denotes |
A quantitative proteomic workflow for characterization of frozen clinical biopsies: laser capture microdissection coupled with label-free mass spectrometry. |
TextSentencer_T2 |
157-365 |
Sentence |
denotes |
This paper describes a simple, highly efficient and robust proteomic workflow for routine liquid-chromatography tandem mass spectrometry analysis of Laser Microdissection Pressure Catapulting (LMPC) isolates. |
T2 |
157-365 |
Sentence |
denotes |
This paper describes a simple, highly efficient and robust proteomic workflow for routine liquid-chromatography tandem mass spectrometry analysis of Laser Microdissection Pressure Catapulting (LMPC) isolates. |
TextSentencer_T3 |
366-559 |
Sentence |
denotes |
Highly efficient protein recovery was achieved by optimization of a "one-pot" protein extraction and digestion allowing for reproducible proteomic analysis on as few as 500 LMPC isolated cells. |
T3 |
366-559 |
Sentence |
denotes |
Highly efficient protein recovery was achieved by optimization of a "one-pot" protein extraction and digestion allowing for reproducible proteomic analysis on as few as 500 LMPC isolated cells. |
TextSentencer_T4 |
560-703 |
Sentence |
denotes |
The method was combined with label-free spectral count quantitation to characterize proteomic differences from 3000-10,000 LMPC isolated cells. |
T4 |
560-703 |
Sentence |
denotes |
The method was combined with label-free spectral count quantitation to characterize proteomic differences from 3000-10,000 LMPC isolated cells. |
TextSentencer_T5 |
704-846 |
Sentence |
denotes |
Significance analysis of spectral count data was accomplished using the edgeR tag-count R package combined with hierarchical cluster analysis. |
T5 |
704-846 |
Sentence |
denotes |
Significance analysis of spectral count data was accomplished using the edgeR tag-count R package combined with hierarchical cluster analysis. |
TextSentencer_T6 |
847-928 |
Sentence |
denotes |
To illustrate the capability of this robust workflow, two examples are presented: |
T6 |
847-928 |
Sentence |
denotes |
To illustrate the capability of this robust workflow, two examples are presented: |
TextSentencer_T7 |
929-1112 |
Sentence |
denotes |
1) analysis of keratinocytes from human punch biopsies of normal skin and a chronic diabetic wound and 2) comparison of glomeruli from needle biopsies of patients with kidney disease. |
T7 |
929-1112 |
Sentence |
denotes |
1) analysis of keratinocytes from human punch biopsies of normal skin and a chronic diabetic wound and 2) comparison of glomeruli from needle biopsies of patients with kidney disease. |
TextSentencer_T8 |
1113-1193 |
Sentence |
denotes |
Differentially expressed proteins were validated by use of immunohistochemistry. |
T8 |
1113-1193 |
Sentence |
denotes |
Differentially expressed proteins were validated by use of immunohistochemistry. |
TextSentencer_T9 |
1194-1426 |
Sentence |
denotes |
These examples illustrate that tissue proteomics carried out on limited clinical material can obtain informative proteomic signatures for disease pathogenesis and demonstrate the suitability of this approach for biomarker discovery. |
T9 |
1194-1426 |
Sentence |
denotes |
These examples illustrate that tissue proteomics carried out on limited clinical material can obtain informative proteomic signatures for disease pathogenesis and demonstrate the suitability of this approach for biomarker discovery. |